• Own the global regulatory roadmap supporting international expansion across key regions (e.g., EU, UK, Canada, China, Japan, Korea, ASEAN, LATAM, Middle East) • Assess regulatory feasibility for new markets, products, and formulations • Develop market entry strategies balancing speed-to-market with compliance and risk • Lead preparation, submission, and maintenance of product registrations, notifications, and approvals globally, with the assistance of consultants as necessary • Oversee technical dossiers, ingredient approvals, and formula assessments per jurisdiction • Manage post-approval lifecycle including renewals, variations, and amendments • Ensure compliance with country-specific import requirements including labeling, claims, customs documentation, tariffs, and certificates • Partner with Supply Chain and Logistics on cross-border compliance, HS codes, COO, COAs, and trade documentation • Support distributor and customs authority interactions where necessary • Monitor evolving global regulatory landscapes affecting dietary supplements, functional foods, nutraceuticals, cosmetics and devices. • Anticipate regulatory changes and proactively adjust strategy • Identify and mitigate regulatory, compliance, and product liability risks • Serve as a strategic advisor to Product Development on globally viable formulations and claims • Collaborate with Quality and Manufacturing on compliance with GMP, audits, required certifications and regulatory inspections • Train internal stakeholders on regulatory requirements and best practices • Act as primary Blueprint representative with global regulatory authorities and external consultants • Build relationships with international regulators, trade associations, and testing bodies • Manage third-party regulatory service providers efficiently and cost-effectively • Build and maintain regulatory SOPs, templates, and internal compliance systems • Ensure documentation supports audits, inspections, and due diligence (including support for M&A or investor reviews)